Feasibility Study to Evaluate Outpatient Blinatumomab in Subjects With Minimal Residual Disease (MRD) of B-precursor Acute Lymphoblastic Leukemia (ALL)
Stopped The decision to terminate is not based on safety or efficacy but due to slow enrollment impacting the ability to complete the study as planned.
Conditions
- B-precursor Acute Lymphoblastic Leukemia
Interventions
- DRUG: Blinatumomab
- DEVICE: Current Wearable Heatlth Monitoring System (CWHMS)
Sponsor
Amgen